Results 171 to 180 of about 94,453 (216)
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Biliary atresia and biliary cysts
Baillière's Clinical Gastroenterology, 1997The authors present a review of the classification, aetiology, presentation, treatment and long-term outcome of children and adults with biliary atresia and choledochal cyst disease. Biliary atresia should be suspected in any infant with jaundice beyond the second week of life.
P A, Lipsett, D L, Segev, P M, Colombani
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Current Opinion in Gastroenterology, 2019
Biliary atresia is a poorly understood deadly disease. Genetic predisposition factors are suspected albeit not firmly established. This review summarizes recent evidence of genetic alterations in biliary atresia.Whole-genome association studies in biliary atresia patients identified four distinct predisposition loci with four different genes ...
Muriel, Girard, Ganna, Panasyuk
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Biliary atresia is a poorly understood deadly disease. Genetic predisposition factors are suspected albeit not firmly established. This review summarizes recent evidence of genetic alterations in biliary atresia.Whole-genome association studies in biliary atresia patients identified four distinct predisposition loci with four different genes ...
Muriel, Girard, Ganna, Panasyuk
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Etiopathogenesis of Biliary Atresia
Seminars in Liver Disease, 2001Biliary atresia, a progressive sclerosis of the extrahepatic biliary tree that occurs only within the first 3 months of life, is one of the most common causes of neonatal cholestasis and accounts for over half of children who undergo liver transplantation.
R J, Sokol, C, Mack
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Biliary atresia in the newborn
Journal of Pediatric Surgery, 1986A prenatal sonographic diagnosis of extrahepatic biliary atresia was made and, 76 hours after birth, operatively confirmed. A standard Kasai operation was performed, with the exception of the use of an ancillary appendiceal conduit to provide biliary drainage of an independent bile duct draining the right anterior hepatic segment.
S K, Greenholz +3 more
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Journal of Pediatric Surgery, 1996
Three infants are described in whom acquired biliary atresia developed during the perinatal period. In two cases this was related to a spontaneous perforation of the bile duct, and in the other it probably was related to previous surgery for duodenal and ileal atresias.
M, Davenport, R, Saxena, E, Howard
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Three infants are described in whom acquired biliary atresia developed during the perinatal period. In two cases this was related to a spontaneous perforation of the bile duct, and in the other it probably was related to previous surgery for duodenal and ileal atresias.
M, Davenport, R, Saxena, E, Howard
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Pediatrics, 1975
It is difficult for me to find fault with Dr. Lilly's presentation, especially since he refers to me as a fair-minded, clear-thinking man! Dr. Thaler and I concluded in 1968 that the chance of encountering a patient with operable atresia of the extrahepatic biliary ducts was so small that our primary obligation was to protect the infant ...
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It is difficult for me to find fault with Dr. Lilly's presentation, especially since he refers to me as a fair-minded, clear-thinking man! Dr. Thaler and I concluded in 1968 that the chance of encountering a patient with operable atresia of the extrahepatic biliary ducts was so small that our primary obligation was to protect the infant ...
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Liver, 2001
Abstract: Although the prognosis of biliary atresia has been improved in recent years, particularly in the era of liver transplantation, hepatic portoenterostomy, e.g., the Kasai operation, is still the first line of surgical treatment. Successful hepatic portoenterostomy depends on early diagnosis and operation, adequate operative technique ...
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Abstract: Although the prognosis of biliary atresia has been improved in recent years, particularly in the era of liver transplantation, hepatic portoenterostomy, e.g., the Kasai operation, is still the first line of surgical treatment. Successful hepatic portoenterostomy depends on early diagnosis and operation, adequate operative technique ...
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Archives of Pediatrics & Adolescent Medicine, 1977
To the Editor.—It is somewhat puzzling to read the recent article on congenital biliary atresia in the August issue of theJournal(130:830,1976) by Kobayashi and co-workers and many others like it in recent literature. In theWestern Journal of Surgery, Obstetrics, and Gynecology(58:714, 1950) there is an article entitled "Surgical Relief of External ...
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To the Editor.—It is somewhat puzzling to read the recent article on congenital biliary atresia in the August issue of theJournal(130:830,1976) by Kobayashi and co-workers and many others like it in recent literature. In theWestern Journal of Surgery, Obstetrics, and Gynecology(58:714, 1950) there is an article entitled "Surgical Relief of External ...
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Current Opinion in Gastroenterology, 1979
This chapter discusses the causes and management of extrahepatic biliary atresia. Extrahepatic biliary atresia, the most common of the progressive hepatic disorders, is itself a rare disease affecting approximately 1: 14,000 live-born infants. It is, nevertheless, the most important hepatic cause of morbidity in infancy and early childhood.
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This chapter discusses the causes and management of extrahepatic biliary atresia. Extrahepatic biliary atresia, the most common of the progressive hepatic disorders, is itself a rare disease affecting approximately 1: 14,000 live-born infants. It is, nevertheless, the most important hepatic cause of morbidity in infancy and early childhood.
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